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PGT-M conditions

This table shows all PGT-M conditions currently approved and awaiting consideration by the HFEA.

Please note that we are updating this database, and some approved conditions may not be displayed. If you are unsure if a condition has been approved or not, please contact pgtm@hfea.gov.uk.

Download full approved condition list.

Condition name Status OMIM number Documents
Keratosis Follicularis Spinulosa Decalvans, X-Linked (KFSDX) approved 308800
Krabbe Disease approved 245200
L–2-Hydroxyglutaric aciduria approved 236792
Lacrimo-auriculo-dento-digital syndrome (LADD) approved 149730
Langers Mesomelic Dysplasia (LMD) approved 249700
Larsen Syndrome approved 150250
Laryngo-onycho-cutaneous (LOC) Syndrome approved 245660
Laurin-Sandrow Syndrome (LSS) approved 135750
Leber congenital amaurosis (LCA) approved 204000, 204100
Leber congenital amaurosis type 10 approved 611755
Leber congenital amaurosis type 12 approved 610612
Leber congenital amaurosis type 13 approved 612712
Leber congenital amaurosis type 14 approved 613341
Leber congenital amaurosis type 15 approved 613843
Leber congenital amaurosis type 16 approved 614186
Leber congenital amaurosis type 17 approved 615360
Leber congenital amaurosis type 3 approved 604232
Leber congenital amaurosis type 4 approved 604393
Leber congenital amaurosis type 5 approved 604537
Leber congenital amaurosis type 6 approved 613826